1-Piperonylpiperazine → HCID 14303517, compound

HRID 1723180Notes

Reaction equation

[O:1]=[C:2]1[C:6]([CH2:13][C:14]([Cl:16])=[O:15])([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:5]2[CH:17]=[CH:18][CH:19]=[CH:20][C:4]=2[O:3]1.[CH2:21]1[O:36][C:35]2[CH:34]=[CH:33][C:25]([CH2:26][N:27]3[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]3)=[CH:24][C:23]=2[O:22]1>>[ClH:16].[O:1]=[C:2]1[C:6]([CH2:13][C:14]([N:30]2[CH2:31][CH2:32][N:27]([CH2:26][C:25]3[CH:33]=[CH:34][C:35]4[O:36][CH2:21][O:22][C:23]=4[CH:24]=3)[CH2:28][CH2:29]2)=[O:15])([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:5]2[CH:17]=[CH:18][CH:19]=[CH:20][C:4]=2[O:3]1

Participants

Reactant 2

HCID 944261-Piperonylpiperazine

HCID 19838007HCID 19838007, compound

Product 1

HCID 14303517HCID 14303517, compound

Procedure

This compound was prepared from 2-(2,3-dihydro-2-oxo-3-phenyl-3-benzofuranyl)acetyl chloride and 4-(3,4-methylenedioxybenzyl)piperazine according to the process described in Example 9.

Sources & evidence

ORD record: ord-de411fc974a24b54bf2e62c9f96c2286
Source dataset: uspto-grants-1989_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04859700

Reaction notes

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